Ink composition, inkjet recording ink and inkjet recording method

ABSTRACT

An ink composition includes a colorant represented by the following formula (I); water; a guanidine-based compound; and a colorless water-soluble planar compound having more than ten delocalized π-electrons within one molecule: 
                         
wherein Pc represents a (k+l+m+n)-valent phthalocyanine nucleus represented by the following formula (II);
 
                         
wherein the symbols in the formulae (I) and (II) are defined in the specification.

TECHNICAL FIELD

The present invention relates to an ink composition containing awater-soluble aromatic compound having an excellent effect on theimprovement of the bronze phenomenon of the recorded image and aguanidine-based compound having an excellent effect on the storagedurability, particularly, gas resistance, of the recorded image, aninkjet recording ink, an inkjet recording method, and a method forimproving both the bronze phenomenon of the inkjet recorded image andthe storage stability of the inkjet recorded image at the same time.

BACKGROUND ART

The inkjet recording method is abruptly overspread and still making aprogress, because the material cost is low, high-speed recording can beperformed, noises are less generated at the recording and colorrecording is easy. The inkjet recording method includes a continuoussystem of continuously flying a liquid droplet and an on-demand systemof flying a liquid droplet according to image information signals, andthe ejection system therefor includes a system of ejecting a liquiddroplet by applying a pressure from a piezoelectric element, a system ofejecting a liquid droplet by generating a bubble in the ink under heat,a system using an ultrasonic wave, and a system of suctioning andejecting a liquid droplet by an electrostatic force. As for the inkjetrecording ink, an aqueous ink, an oil-based ink or a solid (fusion-type)ink is used.

The coloring matter used in such an inkjet recording ink is required toexhibit good solubility in a solvent such as water, enable high-densityrecording, provide a good color hue, be fast to light, heat and activegases in the environment (for example, an oxidative gas such as NOx andozone, and SOx) and highly resistant against water and chemicals, ensuregood fixing property and less blurring on an image-receiving material,give an ink having excellent storability, have high purity and notoxicity and be available at a low cost.

Above all, the coloring matter is strongly demanded to be fast to light,humidity and heat, particularly, at the printing on an image-receivingmaterial having an ink-receiving layer containing a porous whiteinorganic pigment particle, to be fast to oxidative gases such as ozonein the environment and excellent in the water resistance.

On the other hand, in the case where a recorded image having a highoptical density is formed, it is known that there arises a problem thatas the image is dried, the coloring matter crystal deposits on thesurface of the recording material and the recorded image reflects lightto cause a so-called bronze phenomenon of emitting metallic gloss. Thisphenomenon tends to readily occur when the water solubility of thecoloring matter is decreased so as to improve water resistance, lightresistance or gas resistance or a hydrogen bonding group is introducedinto the coloring matter structure. The generation of the bronzephenomenon not only incurs decrease in the optical density of therecorded image but also causes the recorded image to have a color huegreatly different from the desired color hue or lose the transparency.Therefore, it is one of important performances required of the inkjetink to prevent the bronze phenomenon.

As regards the method for preventing the bronze phenomenon, there havebeen heretofore known a method of adding a specific nitrogen-containingcompound (see, for example, JP-A-6-25575 (the term “JP-A” as used hereinmeans an “unexamined published Japanese patent application”),JP-A-6-228476, JP-A-6-248212, JP-A-7-228810, JP-A-7-268261, JP-A-9-12946and JP-A-9-12949), a method of adding a specific heterocyclic compound(see, JP-A-8-259865), a method of adding a specific titanium compound(see, JP-A-8-337745), a method of adding an alkali metal ion (see,JP-A-7-26178), and the like. The bronze phenomenon may be prevented fromoccurring by adding such an additive, but the amount of the additiveadded may be increased because of its insufficient effect or theadditive may decrease various performances of the ink and the quality ofthe recorded image, such as deterioration in the storage stability. Forexample, as described in JP-A-8-259865, when an alkanolamine is added tothe ink, the bronze phenomenon can be prevented, but by the additiononly in a small amount, the pH of the ink increases to 11 or more andthe high pH ink not only adversely affects nozzles but also lacks insafety on erroneously contacting with a human body and moreover,decreases the printing grade or water resistance of the recorded image.

In this way, various effects can be obtained by using an additive, butit is difficult to use conventional additives while maintaining variousperformances. Particularly, in the case where the solubility andaggregating property of the coloring matter need to be taken account of,selection of the kind and amount of the additive is difficult Also, inusing an ionic additive, the effect thereof on the counter ion must alsobe taken into consideration. Accordingly, a molecular design of theadditive by an unconventional new idea and a substantial bronzephenomenon-inhibiting method using the additive are being demanded.

As regards the method for improving such bronze gloss of the recordedimage, there are disclosed a method of using a specific additive incombination (see, for example, JP-A72005-105261), and a method foradding a specific additive in combination for improving the storagestability (particularly, light fastness and ozone gas fastness) of therecorded image (see, for example, JP-A-2006-89730, JP-A-2006-89731,JP-A-2006-89732 and JP-A-2006-89733). However, a method satisfying boththe improvement of bronze phenomenon of the recorded image and theimprovement of preservability of the recorded image at the same time ina high improvement level has not yet been found, and a method for moreimprovement is being demanded at present.

DISCLOSURE OF THE INVENTION

The objects of the present invention are

(1) to provide a novel ink having absorption properties ensuringexcellent color reproduction and at the same time, having sufficientlyhigh fastness to light, heat, humidity and active gas in theenvironment;

(2) to provide an ink of giving a colored image or colored materialexcellent in the color hue and fastness, for example, a printing inkcomposition used in the inkjet recording;

(3) to provide an inkjet recording ink and an inkjet recording method,which can form an image assured of good color hue by the use of aphthalocyanine compound derivative having a specific structure as thecolorant, high fastness to light and active gas in the environment,particularly ozone gas, and excellent water resistance and free ofgeneration of a bronze phenomenon; and

(4) to provide a method satisfying the improvement of both bronzephenomenon and preservability of the image recorded matter at the sametime in a high improvement level by using the above-described inkjetrecording method.

The objects of the present invention can be attained by the followingmeans.

<1> An ink composition comprising:

a colorant represented by the following formula (I);

water;

a guanidine-based compound; and

a colorless water-soluble planar compound having more than tendelocalized π-electrons within one molecule:

wherein,

M represents a hydrogen atom, a metal atom, an oxide thereof, ahydroxide thereof or a halide thereof;

k, l, m and n represent an integer of 0≦k≦8, an integer of 0≦1≦8, aninteger of 0≦m≦8 and an integer of 0≦n≦8, respectively, provided that k,l, m and n satisfy 4≦k+l+m+n≦8;

each of X₁, X₂, X₃ and X₄ represents a substituent selected from thegroup consisting of —SO—R₁, —SO₂—R₁, —SO₂NR₂R₃, —CONR₂R₃, —CO₂—R₁,—CO—R₁, a sulfo group and a salt thereof, a carboxyl group and a saltthereof, and a phosphono group and a salt thereof, provided that atleast one of X₁, X₂, X₃ and X₄ has an ionic hydrophilic group as asubstituent;

R₁ represents a substituted or unsubstituted alkyl group, a substitutedor unsubstituted aryl group, or a substituted or unsubstitutedheterocyclic group;

R₂ represents a hydrogen atom, a substituted or unsubstituted alkylgroup, a substituted or unsubstituted aryl group, or a substituted orunsubstituted heterocyclic group;

R₃ represents a hydrogen atom, a substituted or unsubstituted alkylgroup, a substituted or unsubstituted aryl group, or a substituted orunsubstituted heterocyclic group; and

Pc represents a (k+l+m+n)-valent phthalocyanine nucleus represented bythe following formula (II);

wherein

each of the four benzene rings A, B. C and D has at least one of X₁, X₂,X₃ and X₄; and

Y₁, Y₂, Y₃, Y₄, Y₅, Y₆, Y₇ and Y₈ each independently represents ahydrogen atom or a monovalent substituent which may further have asubstituent.

<2> The ink composition as described in <1>, wherein

the phthalocyanine nucleus represented by the formula (II) isrepresented by the following formula (III):

<3> The ink composition as described in <1> or <2>, wherein

the colorant represented by the formula (I) is represented by thefollowing formula (IV).

wherein

M represents a hydrogen atom, a metal atom, an oxide thereof, ahydroxide thereof or a halide thereof;

k and l represent an integer of 0<k<8 and an integer of 0<l<8,respectively, provided that k and 1 satisfy 4≦k+l≦8;

each of X₁ and X₂ represents a substituent selected from the groupconsisting of —SO—R₁, —SO₂—R₁, —SO₂NR₂R₃, a sulfo group and a saltthereof, provided that X₁ and X₂ are different from each other and atleast one of X₁ and X₂, has an ionic hydrophilic group as a substituent;

R₁ represents a substituted or unsubstituted alkyl group, a substitutedor unsubstituted aryl group, or a substituted or unsubstitutedheterocyclic group;

R₂ represents a hydrogen atom, a substituted or unsubstituted alkylgroup, a substituted or unsubstituted aryl group, or a substituted orunsubstituted heterocyclic group;

R₃ represents a hydrogen atom, a substituted or unsubstituted alkylgroup, a substituted or unsubstituted aryl group, or a substituted orunsubstituted heterocyclic group; and

Pc represents a (k+l)-valent phthalocyanine nucleus represented by theformula (III), wherein

each of the four benzene rings A, B, C and D has at least one of X₁ andX₂.

<4> The ink composition as described in any one of <1> to <3>, wherein

the water-soluble planar compound has at least two aromatic rings.

<5> The ink composition as described in any one of <1> to <4>, wherein

the water-soluble planar compound has no fluorescence, and has 350 nm orless of λ_(max) and 10,000 or less of molar absorption coefficient,wherein

λmax represents a wavelength of the absorption peak having the longestwavelength.

<6> The ink composition as described in any one of <1> to <5>, wherein

the water-soluble planar compound has a sulfo group.

<7> The ink composition as described in any one of <1> to <6>, wherein

the guanidine-based compound is represented by the following formula(1):

R₁₀₁, R₁₀₂, R₁₀₃ and R₁₀₄ each independently represents a hydrogen atom,a substituted or unsubstituted alkyl group, a substituted orunsubstituted alkoxy group, a substituted or unsubstituted aryl group, asubstituted or unsubstituted heterocyclic group, or substituted orunsubstituted an amino group, and

R₁₀₅ represents a hydrogen atom, a substituted or unsubstituted alkylgroup, a substituted or unsubstituted alkoxy group, a substituted orunsubstituted aryl group, or a substituted or unsubstituted heterocyclicgroup.

<8> The ink composition as described in any one of <1> to <7>, wherein

the guanidine-based compound is in an amount of 0.1 to 10 mass % basedon the ink composition.

<9> The ink composition as described in any one of <1> to <8>, furthercomprising:

a surfactant.

<10> The ink composition as described in <9>, wherein

the surfactant is in an amount of 0.05 to 50 g/liter based on the inkcomposition.

<11> The ink composition as described in <9> or <10>, wherein

the surfactant is a nonionic surfactant.

<12> The ink composition as described in <11>, wherein

the nonionic surfactant is an acetylene glycol-based surfactant.

<13> The ink composition as described in any one of <1> to <12>, furthercomprising

an antiseptic.

<14> An inkjet recording ink prepared by using the ink composition asdescribed in any one of <1> to <13>.

<15> An inkjet recording method using the inkjet recording ink asdescribed in <14>.

BEST MODE FOR CARRYING OUT THE INVENTION

The present invention is based on the finding that when a coloranthaving a specific structure represented by formula (I) and a specificcompound are present together, the preservability, particularly, ozoneresistance, of an image can be remarkably enhanced. As well asenhancement of the ozone resistance, an image quality free of bronzegloss, bleeding or beading can also be ensured.

The constituent elements of the present invention are described indetail below, (Colorant Represented by Formula (I) or (II))

The colorant for use in the present invention is a phthalocyaninederivative having a specific structure (a specific number of specificsubstituents are introduced into specific substitution sites), and ithas been found that by virtue of using this colorant, thepreservability, particularly, ozone gas resistant fastness, of therecorded image can be greatly enhanced.

That is, the phthalocyanine derivative having a specific structure,which is the colorant for use in the present invention represented byformula (I) or (II), is greatly characterized by controlling theposition of the substituent at the molecular synthesis to havesubstituents (X₁, X₂, X₃ and X₄) only at the β-position of the benzenering in the phthalocyanine skeleton.

The phthalocyanine derivative usually has a substituent such aswater-soluble group randomly at the α-position (to describe by referringto the phthalocyanine molecule of the present invention, this positionincludes the substitution sites of Y₁, Y₂, Y₃, Y₄, Y₅, Y₆, Y₇ and Y₈)and the β-position (to describe by referring to the phthalocyaninemolecule of the present invention, this position includes thesubstitution sites of X₁, X₂, X₃ and X₄ to four benzene rings A, B, Cand D of the phthalocyanine molecule as the mother nucleus) of fourbenzene rings of the phthalocyanine skeleton.

The phthalocyanine derivative as the colorant for use in the presentinvention has, as described above, a specific number of specificsubstituents only at the β-position, and this construction is consideredto provide an effect of promoting the aggregation of phthalocyaninemolecules and at the same time, enhancing the oxidation potential,thereby ensuring excellent weather resistance (light fastness, gasresistance).

The colorant for use in the present invention is preferably aphthalocyanine derivative having a structure represented by thefollowing formula (I).

The colorant represented by formula (I) or (II) for use in the presentinvention includes a sole phthalocyanine derivative dye, and a dyemixture or a salt or hydrate thereof. The salts or hydrates may be usedindividually or as a mixture in the colorant.

In formula (I), M represents a hydrogen atom, a metal atom or an oxide,hydroxide or halide thereof.

Examples of the metal atom include Li, Na, K, Mg, Ti, Zr, V, Nb, Ta, Cr,Mo, W, Mn, Fe, Co, Ni, Ru, Rh, Pd, Os, Ir, Pt, Cu, Ag, Au, Zn, Cd, Hg,Al, Ga, In, Si, Ge, Sn, Pb, Sb and Bi.

Examples of the oxide include VO and GeO.

Examples of the hydroxide include Si(OH)₂, Cr(OH)₂ and Sn(OH)₂.

Examples of the halide include AlCl, SiCl₂, VCl, VCl₂, VOCl, FeCl, GaCland ZrCl.

Above all, M is preferably Cu, Ni, Zn, Al or the like, and mostpreferably Cu.

In formula (I), X₁, X₂, X₃ and X₄ each independently represents asubstituent selected from —SO—R₁, —SO₂—R₁, —SO₂NR₂R₃, —CONR₂R₃, —CO₂—R₁,—CO—R₁, a sulfo group and a salt thereof, a carboxyl group and a saltthereof, and a phosphono group and a salt thereof and at the same time,at least one of the substituents is present in each of four benzenerings {A, B, C and D in formula (II)} of the phthalocyanine nucleus.

X₁, X₂, X₃ and X₄ each is independently preferably —SO—R₁, —SO₂—R₁,—SO₂NR₂R₃, —CONR₂R₃, —CO₂—R^(X), or —CO—R₁, more preferably —SO₂—R₁, or—SO₂NR₂R₃, and most preferably —SO₂—R₁.

Here, at least one of X₁, X₂, X₃ and X₄ has an ionic hydrophilic groupas a substituent.

Examples of the ionic hydrophilic group include a sulfo group, acarboxyl group, a phosphono group and a quaternary ammonium group. Amongthese, a carboxyl group, a phosphono group and a sulfo group arepreferred, and a carboxyl group and a sulfo group are more preferred.The carboxyl group, phosphono group and sulfo group each may be in thestate of a salt. Examples of the counter ion forming the salt include anammonium ion, an alkali metal ion (e.g., lithium ion, sodium ion,potassium ion) and an organic cation (e.g., tetramethylammonium ion,tetramethyl-guanidium ion, tetramethylphosphonium ion). Among thesecounter ions, an alkali metal salt is preferred, and a lithium salt ismore preferred, because the solubility of dye and the stability of inkare enhanced,

R₁ is preferably a substituted or unsubstituted alkyl group, asubstituted or unsubstituted aryl group or a substituted orunsubstituted heterocyclic group, and most preferably a substitutedalkyl group, a substituted aryl group or a substituted heterocyclicgroup.

R₂ is preferably a hydrogen atom, a substituted or unsubstituted alkylgroup, a substituted or unsubstituted aryl group or a substituted orunsubstituted heterocyclic group, more preferably a hydrogen atom, asubstituted alkyl group or a substituted aryl group, still morepreferably a hydrogen atom or a substituted alkyl group, and mostpreferably a hydrogen atom,

R₃ is preferably a hydrogen atom, a substituted or unsubstituted alkylgroup, a substituted or unsubstituted aryl group or a substituted orunsubstituted heterocyclic group, more preferably a hydrogen atom, asubstituted alkyl group, a substituted aryl group or a substitutedheterocyclic group, still more preferably a substituted alkyl group or asubstituted aryl group, and most preferably a substituted alkyl group.

The substituted or unsubstituted alkyl group represented by R₁, R₂ andR₃ is preferably an alkyl group having a carbon number of 1 to 12. Thealkyl group is more preferably a branched alkyl group, still morepreferably an alkyl group having an asymmetric carbon (use in theracemic form), because the solubility of dye and the stability of inkare enhanced.

Examples of the substituent are the same as those of the substituentdescribed later when R₁, R₂, R₃ and Y each may further have asubstituent. In particular, a hydroxyl group, an ether group, an estergroup, a cyano group, an amido group and a sulfonamido group arepreferred, because the aggregating property of dye and the fastness areenhanced. Other than these, the alkyl group may have a halogen atom oran ionic hydrophilic group.

The substituted or unsubstituted cycloalkyl group represented by R₁, R₂and R₃ is preferably a cycloalkyl group having a carbon number of 5 to12, The cycloalkyl group is more preferably a cycloalkyl group having anasymmetric carbon (use in the racemic form), because the solubility ofdye and the stability of ink are enhanced.

Examples of the substituent are the same as those of the substituentdescribed later when R₁, R₂, R₃ and Y each may further have asubstituent. In particular, a hydroxyl group, an ether group, an estergroup, a cyano group, an amido group and a sulfonamido group arepreferred, because the aggregating property of dye and the fastness areenhanced. Other than these, the cycloalkyl group may have a halogen atomor an ionic hydrophilic group.

The substituted or unsubstituted alkenyl group represented by R₁, R₂ andR₃ is preferably an alkenyl group having a carbon number of 2 to 12. Thealkenyl group is more preferably a branched alkenyl group, still morepreferably an alkenyl group having an asymmetric carbon (use in theracemic form), because the solubility of dye and the stability of inkare enhanced.

Examples of the substituent are the same as those of the substituentdescribed later when R₁, R₂, R₃ and Y each may further have asubstituent. In particular, a hydroxyl group, an ether group, an estergroup, a cyano group, an amido group and a sulfonamido group arepreferred, because the aggregating property of dye and the fastness areenhanced, Other than these, the alkenyl group may have a halogen atom oran ionic hydrophilic group.

The substituted or unsubstituted aralkyl group represented by R₁, R₂ andR₃ is preferably an aralkyl group having a carbon number of 7 to 18. Thearalkyl group is more preferably a branched aralkyl group, still morepreferably an aralkyl group having an asymmetric carbon (use in theracemic form), because the solubility of dye and the stability of inkare enhanced.

Examples of the substituent are the same as those of the substituentdescribed later when R₁, R₂, R₃ and Y each may further have asubstituent. In particular, a hydroxyl group, an ether group, an estergroup, a cyano group, an amido group and a sulfonamido group arepreferred, because the aggregating property of dye and the fastness areenhanced. Other than these, the aralkyl group may have a halogen atom oran ionic hydrophilic group.

The substituted or unsubstituted aryl group represented by R₁, R₂ and R₃is preferably an aryl group having a carbon number of 6 to 12.

Examples of the substituent are the same as those of the substituentdescribed later when R₁, R₂, R₃ and Y each may further have asubstituent. Among these, an electron-withdrawing group is preferred,because the oxidation potential of the dye becomes noble and thefastness is enhanced. In particular, a halogen atom, a hetero group, acyano group, a carboxyl group, an acylamino group, a sulfonamido group,a sulfamoyl group, a carbamoyl group, a sulfonyl group, an imido group,an acyl group, a sulfo group and a quaternary ammonium group arepreferred, and a cyano group, a carboxyl group, a sulfamoyl group, acarbamoyl group, a sulfonyl group, an imido group, an acyl group, asulfo group and a quaternary ammonium group are more preferred.

The heterocyclic group represented by R₁, R₂ and R₃ preferably has a 5-or 6-membered ring, and such a ring may be further ring-condensed. Also,the heterocyclic group may be an aromatic heterocyclic group or anon-aromatic heterocyclic group.

Examples of the heterocyclic group represented by R₁, R₂ and R₃ aredescribed below in the form of a hetero ring by omitting thesubstitution site, but the substitution site is not limited and, forexample, pyridine can be substituted at the 2-position, 3-position or4-position. Examples of the heterocyclic group include pyridine,pyrazine, pyrimidine, pyridazine, triazine, quinoline, isoquinoline,quinazoline, cinnoline, phthalazine, quinoxaline, pyrrole, indole,furan, benzofuran, thiophene, benzothiophene, pyrazole, imidazole,benzimidazole, triazole, oxazole, benzoxazole, thiazole, benzothiazole,isothiazole, benzisothiazole, thiadiazole, isoxazole, benzisoxazole,pyrrolidine, piperidine, piperazine, imidazoline and thiazoline.

Above all, the heterocyclic group is preferably an aromatic heterocyclicgroup. Preferred examples thereof include, as denoted in the same manneras above, pyridine, pyrazine, pyrimidine, pyridazine, triazine,pyrazole, imidazole, benzimidazole, triazole, thiazole, benzothiazole,isothiazole, benzisothiazole and thiadiazole.

These groups each may have a substituent, and examples of thesubstituent are the same as those of the substituent described laterwhen R₁, R₂, R₃ and Y each may further have a substituent.

Preferred substituents are the same as preferred substituents of thearyl group above, and more preferred substituents are the same as morepreferred substituents of the aryl group above,

In formula (II), Y₁, Y₂, Y₃, Y₄, Y₅, Y₆, Y₇ and Y₈ each independentlyrepresents a hydrogen atom or a monovalent substituent, and themonovalent substituent may further have a substituent.

Examples of the monovalent substituent represented by Y₁, Y₂, Y₃, Y₄,Y₅, Y₆, Y₇ and Y₈ include a halogen atom, an alkyl group, an alkenylgroup, an aralkyl group, an aryl group, a heterocyclic group, a cyanogroup, a hydroxyl group, a nitro group, an amino group, an alkylaminogroup, an alkoxy group, an aryloxy group, an amido group, an arylaminogroup, a ureido group, a sulfamoylamino group, an alkylthio group, anarylthio group, an alkoxycarbonylamino group, a sulfonamido group, acarbamoyl group, an alkoxycarbonyl group, a heterocyclic oxy group, anazo group, an acyloxy group, a carbamoyloxy group, a silyloxy group, anaryloxycarbonyl group, an aryloxycarbonylamino group, an imido group, aheterocyclic thio group, a phosphoryl group and an acyl group. Thesegroups each may further have a substituent,

Y₁ to Y₈ each is preferably a hydrogen atom, a halogen atom, an alkylgroup, an aryl group, a cyano group, an alkoxy group, an amido group, aureido group, a sulfonamido group, a carbamoyl group, a sulfamoyl groupor an alkoxycarbonyl group, more preferably a hydrogen atom, a halogenatom or a cyano group, and most preferably a hydrogen atom. The numberof carbon atoms in the monovalent substituent is preferably less than 8.

Incidentally, when R₁, R₂, R₃ and Y (Y₁ to Y₈) each is a group which mayfurther have a substituent, the group may further have a substituentdescribed below.

The substituent includes a linear or branched alkyl group having acarbon number of 1 to 12, a linear or branched aralkyl group having acarbon number of 7 to 18, a linear or branched alkenyl group having acarbon number of 2 to 12, a linear or branched alkynyl group having acarbon number of 2 to 12, a linear or branched cycloalkyl group having acarbon number of 3 to 12, a linear or branched cycloalkenyl group havinga carbon number of 3 to 12 (these groups each is preferably a grouphaving a branched chain, more preferably a group having an asymmetriccarbon, because the solubility of dye and the stability of ink areenhanced; e.g., methyl, ethyl, propyl, isopropyl, sec-butyl, tert-butyl,2-ethylhexyl, 2-methylsulfonylethyl, 3-phenoxypropyl, trifluoromethyl,cyclopentyl), a halogen atom (e.g., chlorine, bromine), an aryl group(e.g., phenyl, 4-tert-butylphenyl, 2,4-di-tert-amylphenyl), aheterocyclic group (e.g., imidazolyl, pyrazolyl, triazolyl, 2-furyl,2-thienyl, 2-pyrimidinyl, 2-benzothiazolyl), a cyano group, a hydroxylgroup, a nitro group, a carboxy group, an amino group, an alkyloxy group(e.g., methoxy, ethoxy, 2-methoxyethoxy, 2-methanesulfonylethoxy), anaryloxy group (e.g., phenoxy, 2-methylphenoxy, 4-tert-butylphenoxy,3-nitrophenoxy, 3-tert-butyloxycarbamoylphenoxy, 3-methoxy-carbamoyl),an acylamino group (e.g., acetamido, benzamido,4-(3-tert-butyl-4-hydroxyphenoxy)butanamido), an alkylamino group (e.g.,methylamino, butylamino, diethylamino, methylbutylamino), an arylaminogroup (e.g., phenylamino, 2-chloroanilino), a ureido group (e.g.,phenylureido, methylureido, N,N-dibutylureido), a sulfamoylamino group(e.g., N,N-dipropylsulfamoylamino), an alkylthio group (e.g.,methylthio, octylthio, 2-phenoxyethylthio), an arylthio group (e.g.,phenylthio, 2-butoxy-5-tert-octylphenylthio, 2-carboxyphenylthio), analkyloxycarbonylamino group (e.g., methoxycarbonylamino), a sulfonamidogroup (e.g., methanesulfonamido, benzenesulfonamido,p-toluenesulfonamido), a carbamoyl group (e.g., N-ethylcarbamoyl,N,N-dibutylcarbamoyl), a sulfamoyl group (e.g., N-ethylsulfamoyl,N,N-dipropylsulfamoyl, N-phenylsulfamoyl), a sulfonyl group (e.g.,methanesulfonyl, octanesulfonyl, benzenesulfonyl, toluenesulfonyl), analkyloxycarbonyl group (e.g., methoxycarbonyl, butyloxycarbonyl), aheterocyclic oxy group (e.g., 1-phenyltetrazol-5-oxy,2-tatrahydropyranyloxy), an azo group (e.g., phenylazo,4-methoxyphenylazo, 4-pivaloylaminophenylazo,2-hydroxy-4-propanoylphenylazo), an acyloxy group (e.g., acetoxy), acarbamoyloxy group (e.g., N-methylcarbamoyloxy, N-phenylcarbamoyloxy), asilyloxy group (e.g., trimethylsilyloxy, dibutylmethylsilyloxy), anaryloxycarbonylamino group (e.g., phenoxycarbonylamino), an imido group(e.g., N-succinimido, N-phthalimido), a heterocyclic thio group (e.g.,2-benzothiazolylthio, 2,4-di-phenoxy-1,3,5-triazole-6-thio,2-pyridylthio), a sulfinyl group (e.g., 3-phenoxypropylsulfinyl), aphosphonyl group (e.g., phenoxyphosphonyl, octyloxyphosphonyl,phenylphosphonyl), an aryloxycarbonyl group (e.g., phenoxycarbonyl), anacyl group (e.g., acetyl, 3-phenylpropanoyl, benzoyl), and an ionichydrophilic group (e.g., carboxyl, sulfo, phosphono, quaternaryammonium).

In formula (I), k, l, m and n represent an integer of 0≦k≦8, an integerof 0≦l≦8, an integer of 0≦m≦8 and an integer of 0≦n≦8.

Here, k, l, m and n each represents a number satisfying 4≦k+l+m+n≦8.

k, l, m and n are preferably an integer of 0<k<8, an integer of 0<l<8,an integer of 0≦m<8 and n=0, more preferably an integer of 0<k<8, aninteger of 0<l<8, and m=n=0, and most preferably an integer of 0<k<4, aninteger of 0<l<4 (represents a number satisfying k+l=4), and m=n=0

Preferred combinations as the colorant represented by formula (I) (or(II)) are summarized as follows.

(a) X₁, X₂, X₃ and X₄ each is independently preferably —SO—R₁, —SO₂—R₁,—SO₂NR₂R₃, —CONR₂R₃, —CO₂—R₁, or —CO—R₁, more preferably —SO₂—R₁,—SO₂NR₂R₃, —CONR₂R₃, —CO₂—R₁, or —CO—R₁, still more preferably —SO₂—R₁or —SO₂NR₂R₃, and most preferably —SO₂—R₁.

(b) R₁ is a substituted or unsubstituted alkyl group, a substituted orunsubstituted aryl group or a substituted or unsubstituted heterocyclicgroup, preferably a substituted alkyl group, a substituted aryl group ora substituted heterocyclic group, and most preferably a substitutedalkyl group having an ionic hydrophilic group and/or a hydroxyl group asa substituent.

(c) R₂ is a hydrogen atom, a substituted or unsubstituted alkyl group, asubstituted or unsubstituted aryl group or a substituted orunsubstituted heterocyclic group, preferably a hydrogen atom, asubstituted alkyl group, a substituted aryl group or a substitutedheterocyclic group, and most preferably a hydrogen atom.

(d) R₃ is a hydrogen atom, a substituted or unsubstituted alkyl group, asubstituted or unsubstituted aryl group or a substituted orunsubstituted heterocyclic group, preferably a substituted alkyl group,a substituted aryl group or a substituted heterocyclic group, and mostpreferably a substituted alkyl group having an ionic hydrophilic groupand/or a hydroxyl group as a substituent.

(e) M is preferably Cu, Ni, Zn, Al or the like, and most preferably Cu.

(f) Y₁ to Y₈ each is independently preferably a hydrogen atom or ahalogen atom, and most preferably a hydrogen atom

(g) In the colorant for use in the present invention, the phthalocyaninenucleus represented by formula (II) is preferably represented by thefollowing formula (III):

(h) The average molecular weight of the phthalocyanine derivative as thecolorant for use in the present invention is preferably from 750 to2,500, more preferably from 995 to 2,500, still more preferably from 995to 2,000, and most preferably from 995 to 1,800.

(i) Among the colorants represented by formula (I), a colorant having atleast one ionic hydrophilic group per one unit of the phthalocyaninenucleus is preferred, a colorant where the ionic hydrophilic group is asulfo group is more preferred, and a colorant having two or more sulfogroups is most preferred,

(j) As for the number of ionic hydrophilic groups contained in thephthalocyanine derivative as the colorant represented by formula (I) ofthe present invention, those having at least one ionic hydrophilic groupwithin one molecule of the phthalocyanine derivative are preferred,those having two or more ionic hydrophilic groups are more preferred,and those having at least two or more sulfo groups and/or carboxylgroups are most preferred because of their good solubility ordispersibility in an aqueous medium.

(j) As for the preferred combination of substituents in the colorantrepresented by formula (I) of the present invention, a compound where atleast one of various substituents is the preferred group is preferred, acompound where a larger number of various substituents are the preferredgroups is more preferred, and a compound where all substituents are thepreferred groups is most preferred.

Among the colorants represented by formula (I) for use in the presentinvention, a phthalocyanine derivative having a structure represented bythe following formula (IV) is more preferred.

The colorant represented by formula (IV) (or (III)) for use in thepresent invention includes a sole phthalocyanine derivative dye, and adye mixture or a salt or hydrate thereof. The salts or hydrates may beused individually or as a mixture in the colorant.

In formula (IV), M represents a hydrogen atom, a metal atom or an oxide,hydroxide or halide thereof.

Pc represents a (k+l)-valent phthalocyanine nucleus represented by thefollowing formula (III)

In formula (IV), M, X₁ and X₂ each independently has the same meaning asM, X₁ or X₂ in formula (I), and preferred examples are also the same.

In formula (IV), k and l represent an integer of 0<k<8 and an integer of0<l<8, provided that k and 1 each represents a number satisfying4≦k+l≦8.

k and l represent an integer of 0<k<8 and an integer of 0<l<8, and mostpreferably an integer of 0<k<4 and an integer of 0<l<4 (k and 1 eachrepresents a number satisfying k+l=4).

Preferred combinations as the colorant represented by formulae (IV) and(III) are summarized as follows.

(a) X₁ and X₂ each is independently preferably —SO—R₁, —SO₂—R₁,—SO₂NR₂R₃, —CONR₂R₃, —CO₂—R₁ or —CO—R₁, more preferably —SO₂—R₁,—SO₂NR₂R₃, —CONR₂R₃, —CO₂—R₁, or —CO—R₁, still more preferably —SO₂—R₁or —SO₂NR₂R₃, and most preferably —SO₂—R₁.

(b) R₁ is a substituted or unsubstituted alkyl group, a substituted orunsubstituted aryl group or a substituted or unsubstituted heterocyclicgroup, preferably a substituted alkyl group, a substituted aryl group ora substituted heterocyclic group, and most preferably a substitutedalkyl group having an ionic hydrophilic group and/or a hydroxyl group asa substituent,

(c) R₂ is a hydrogen atom, a substituted or unsubstituted alkyl group, asubstituted or unsubstituted aryl group or a substituted orunsubstituted heterocyclic group, preferably a hydrogen atom, asubstituted alkyl group, a substituted aryl group or a substitutedheterocyclic group, and most preferably a hydrogen atom.

(d) R₃ is a hydrogen atom, a substituted or unsubstituted alkyl group, asubstituted or unsubstituted aryl group or a substituted orunsubstituted heterocyclic group, preferably a substituted alkyl group,a substituted aryl group or a substituted heterocyclic group, and mostpreferably a substituted alkyl group having an ionic hydrophilic groupand/or a hydroxyl group as a substituent.

(e) M is preferably Cu, Ni, Zn, Al or the like, and most preferably Cu.

(f) The average molecular weight of the phthalocyanine derivative as thecolorant for use in the present invention is preferably from 750 to2,500, more preferably from 995 to 2,500, still more preferably from 995to 2,000, and most preferably from 995 to 1,800.

(g) Among the colorants represented by formula (IV), a colorant havingat least one ionic hydrophilic group per one unit of the phthalocyaninenucleus is preferred, a colorant where the ionic hydrophilic group is asulfo group is more preferred, and a colorant having two or more sulfogroups is most preferred.

(h) As for the number of ionic hydrophilic groups contained in thephthalocyanine derivative as the colorant represented by formula (IV) or(III) of the present invention, those having at least one ionichydrophilic group within one molecule of the phthalocyanine derivativeare preferred, those having two or more ionic hydrophilic groups aremore preferred, and those having at least two or more sulfo groupsand/or carboxyl groups are most preferred because of their goodsolubility or dispersibility in an aqueous medium.

As for the preferred combination of substituents in the colorantrepresented by formula (IV) of the present invention, a compound whereat least one of various substituents is the preferred group ispreferred, a compound where a larger number of various substituents arethe preferred groups is more preferred, and a compound where allsubstituents are the preferred groups is most preferred.

In general, the inkjet recording ink is known to use variousphthalocyanine compounds. The phthalocyanine compound represented by thefollowing formula (X) sometimes contains an isomer with respect to thesubstitution site of the substituent R^(n) (n=1 to 16) (here, R¹ to R¹⁶are defined as substituents at 1-position to 16-position, respectively),which inevitably occurs at the time of synthesis, but these substitutionsite isomers are not distinguished from each other but regarded as thesame derivative in many cases. Also, in the case where the substituent Rcontains an isomer, these are not distinguished but regarded as the samephthalocyanine compound in many cases.

To describe the definition in the present invention by referring toformula (X), the case where the structure of the phthalocyanine compoundis different indicates a case where the constituent atom species of thesubstituent R^(n) (n=1 to 16) is different, a case where the number ofsubstituents R^(n) is different, or a case where the positions of thesubstituents R^(n) are different.

In the present invention, the derivatives differing in the structure ofthe phthalocyanine compound represented by formula (X) (particularly,the substitution site) are defined by classifying these into thefollowing three groups.

(1) β-Position substitution type: (a phthalocyanine compound havingspecific substituents at the 2- and/or 3-position, the 6- and/or7-position, the 10- and/or 11-position, and the 14- and/or 15-position)

(2) α-Position substitution type: (a phthalocyanine compound havingspecific substituents at the 1- and/or 4-position, the 5- and/or8-position, the 9- and/or 12-position, and the 13- and/or 16-position)

(3) α,β-Position mixed substitution type: (a phthalocyanine compoundhaving specific substitutions at the 1- to 16-positions without anyregularity)

In the present invention, phthalocyanine derivatives differing in thestructure (particularly, the substitution site) are described by usingthese (1) β-position substitution type, (2) α-position substitution typeand (3) α,β-position mixed substitution type.

The obtained phthalocyanine derivative (for example, when k=l=m=n=1) isusually a mixture of compounds represented by the following formulae(a)−1 to (a)−4 which are isomers with respect to the introduction siteof each of the substituents G₁, G₂, G₃ and G₄ (common in that theintroduction site is the β-position).

That is, the compounds represented by formulae (a)−1 to (a)−4 are theβ-position substitution type (a phthalocyanine compound having specificsubstituents at the 2- and/or 3-position, the 6- and/or 7-position, the10- and/or 11-position, and the 14- and/or 15-position) and arecompounds utterly differing in the structure (different in theintroduction site of specific substituents) from the α-positionsubstitution type (a phthalocyanine compound having specificsubstituents at the 1- and/or 4-position, the 5- and/or 8-position, the9- and/or 12-position, and the 13- and/or 16-position) and theα,β-position mixed substitution type (a phthalocyanine compound havingspecific substitutions at the 1- to 16-positions without anyregularity), This is a structural feature very important as means forachieving the objects of the present invention.

The detailed reasons why the problems to be solved by the presentinvention have been overcome are not known, but a derivative where asoluble group is introduced only into the β-position tends to be by farexcellent in the color hue, light fastness, ozone gas resistance and thelike as compared with other derivatives.

More specifically, the phthalocyanine compound for use in the presentinvention having [1] a good spectral absorption property (aggregation ofthe phthalocyanine compound is accelerated by virtue of introduction ofa specific soluble group into the β-position), [2] high image fastness(by virtue of high oxidation potential and acceleration of strongaggregation, for example, color fading by an oxidation reaction betweenthe phthalocyanine compound and the ozone gas as an electrophilicreagent is suppressed), [3] high solubility in the ink composition, and[4] an ability of giving an ink solution with good aging stability, isconsidered to be achieved by introducing a specific number of specificsoluble groups into a specific position (β-position), that is, enablingto form a firm aggregate of a completely β-position substitution-typephthalocyanine compound having high oxidation potential and at the sametime, selectively introduce only an objective number of specific solublegroups.

Specific examples (Dyes 1 to 160) of the colorant for use in the presentinvention are set forth below, but the present invention is limited tothese specific examples.

In Table 1 below, formula (XX-1) represents a (k)-valent phthalocyaninenucleus (the introduction site of the substituent R is the β-positionsubstitution type defined in the present invention), t represents anumber of t=1 or 2, and k represents a number satisfying 4≦k≦8.

TABLE 1 Formula (XX-1):

Compound No. M R₁ k 101 Cu —SO₂—(CH₂)₃—SO₃Li 4 102 Cu

4 103 Cu —SO₂—(CH₂)₆—CO₂Na 4 104 Cu

4 105 Cu

4 M-Pc-(R)_(k) In the Table, introduction sites of respectivesubstituents of (R) are in an irregular order within the β-positionsubstitution type [showing isomers represented by formulae (a)-1 to(a)-4]. The value of k is a charging ratio (eq./eq.) of thephthalonitrile derivative used in the synthesis of the phthalocyaninederivative.

In Tables 2 to 10 below, formula (XX-2) represents a (k+l)-valentphthalocyanine nucleus (the introduction site of the substituent R₁ isthe β-position substitution type defined in the present invention), Rrepresents R₁ and/or R₂, t represents a number of t=1 or 2, k representsa number of 4≦k≦8, and 1 represents a number of 0<l<8, provided that kand l each represents a number satisfying 4≦k+l≦8.

TABLE 2 Formula (XX-2):

Compound No. M R₁ k R₂ l 106 Cu —SO—(CH₂)₃—SO₃K 3—SO₂(CH₂)₃—SO₂NH—C₂H₄OC₂H₄OH 1 107 Cu —SO₂—(CH₂)₃—SO₃K 2—SO₂(CH₂)₃—SO₂NH—C₂H₄OC₂H₄OH 2 108 Cu —SO₂—(CH₂)₃—SO₃Li 3

1 109 Cu —SO₂—(CH₂)₃—SO₃Li 2.7

1.3 110 Cu —SO₂—(CH₂)₃—SO₃Li 2

2

In the Table, introduction sites of respective substituents of (R₁) and(R₂) are in an irregular order within the β-position substitution type[showing isomers represented by formulae (a)-1 to (a)-4]. The value of kand l are a charging ratio (eq./eq.) of the phthalonitrile derivativeused in the synthesis of the phthalocyanine derivative.

TABLE 3 Compound No. M R₁ k R₂ l 111 Cu —SO₂—(CH₂)₃—SO₃Li 3.33

0.67 112 Cu —SO₂—(CH₂)₃—SO₃Li 3.50

0.50 113 Cu —SO₂—(CH₂)₃—SO₃Li 3

1 114 Cu —SO₂—(CH₂)₃—SO₃Li 3

1 115 Cu —SO₂—(CH₂)₃—SO₃Li 3

1

In the Table, introduction sites of respective substituents of (R₁) and(R₂) are in an irregular order within the β-position substitution type[showing isomers represented by formulae (a)-1 to (a)-4]. The value of kand l are a charging ratio (eq./eq.) of the phthalonitrile derivativeused in the synthesis of the phthalocyanine derivative.

TABLE 4 Compound No. M R₁ k R₂ l 116 Cu —SO₂—(CH₂)₄—SO₃Li 3—SO₂—(CH₂)₃—SO₂NH—C₂H₄OC₂H₄OH 1 117 Cu

3 —SO₂—(CH₂)₃—SO₂NH—C₂H₄OC₂H₄OH 1 118 Cu —SO₂—(CH₂)₃—CO₂Li 3

1 119 Cu —SO₂—(CH₂)₃—CO₂Li 2

2 120 Cu —SO₂—(CH₂)₃—CO₂Li 3

1

In the Table, introduction sites of respective substituents of (R₁) and(R₂) are in an irregular order within the β-position substitution type[showing isomers represented by formulae (a)-1 to (a)-4]. The value of kand l are a charging ratio (eq./eq.) of the phthalonitrile derivativeused in the synthesis of the phthalocyanine derivative.

TABLE 5 Compound No. M R₁ k R₂ l 121 Cu —SO₂—(C₂H₄O)—C₂H₄SO₃Li 3

1 122 Cu —SO₂—(C₂H₄O)₂—C₂H₄SO₃Li 3

1 123 Cu —SO₂—(C₂H₄O)₃—C₂H₄SO₃Li 2

2 124 Cu —SO₂—(CH₂)₃—SO₃Li 2 —SO₂—(C₂H₄O)₂—C₂H₄OH 2 125 Cu—SO₂—(CH₂)₃—SO₃Li 2 —SO₂—(C₂H₄O)₂—C₂H₄OCH₃ 2

In the Table, introduction sites of respective substituents of (R₁) and(R₂) are in an irregular order within the β-position substitution type[showing isomers represented by formulae (a)-1 to (a)-4]. The value of kand l are a charging ratio (eq./eq.) of the phthalonitrile derivativeused in the synthesis of the phthalocyanine derivative.

TABLE 6 Compound No. M R₁ k R₂ l 126 Cu —SO₂—(CH₂)₃—SO₃K 1

3 127 Cu —SO₂—(CH₂)₃—SO₃Li 3 —SO₂—(CH₂)₃—CO₂Li 1 128 Cu—SO₂—(CH₂)₃—SO₃Li 3 —SO₂—(CH₂)₅—CO₂Li 1 129 Cu —SO₂—(CH₂)₃—SO₃Li 1

3 130 Cu

3

1

In the Table, introduction sites of respective substituents of (R₁) and(R₂) are in an irregular order within the β-position substitution type[showing isomers represented by formulae (a)-1 to (a)-4]. The value of kand l are a charging ratio (eq./eq.) of the phthalonitrile derivativeused in the synthesis of the phthalocyanine derivative.

TABLE 7 Compound No. M R₁ k R₂ l 131 Cu —SO₂—(CH₂)₃—SO₃Li 1

3 132 Ni —SO₂—(CH₂)₄—SO₃Li 1

3 133 Zn

1

3 134 Cu

1

3 135 Cu

2

2

In the Table, introduction sites of respective substituents of (R₁) and(R₂) are in an irregular order within the β-position substitution type[showing isomers represented by formulae (a)-1 to (a)-4]. The value of kand l are a charging ratio (eq./eq.) of the phthalonitrile derivativeused in the synthesis of the phthalocyanine derivative.

TABLE 8 Compound No. M R₁ k R₂ l 136 Cu —SO₂—(CH₂)₃—SO₃Li 3

1 137 Cu —SO₂—(CH₂)₃—SO₃Li 2

2 138 Cu

1

3 139 Cu

3

1 140 Cu

2

2

In the Table, introduction sites of respective substituents of (R₁) and(R₂) are in an irregular order within the β-position substitution type[showing isomers represented by formulae (a)-1 to (a)-4]. The value of kand l are a charging ratio (eq./eq.) of the phthalonitrile derivativeused in the synthesis of the phthalocyanine derivative.

TABLE 9 Compound No. M R₁ k R₂ l 141 Cu —SO₂NH₂—(CH₂)₂—SO₃K 3

1 142 Cu —SO₂NH₂—(CH₂)₃—SO₃Li 3

1 143 Cu

3 —SO₂NH₂—C₂H₄OC₂H₄OH 1 144 Cu

3

1 145 Cu —SO₂—(CH₂)₃—SO₃Li 3

1

In the Table, introduction sites of respective substituents of (R₁) and(R₂) are in an irregular order within the β-position substitution type[showing isomers represented by formulae (a)-1 to (a)-4]. The value of kand l are a charging ratio (eq./eq.) of the phthalonitrile derivativeused in the synthesis of the phthalocyanine derivative.

TABLE 10 Compound No. M R₁ k R₂ l 146 Cu —SO₂—(CH₂)₃—SO₃Li 3—CONH—C₂H₄OC₂H₄OH 1 147 Cu —SO₂—(CH₂)₃—SO₃Li 2.4

1.6 148 Cu —SO₂—(CH₂)₃—SO₃Li 3 —CO₂—C₂H₄OC₂H₄OC₂H₄SO₃Li 1 149 Cu

3 —CO—CH₃ 1 150 Cu —SO₂NH—C₂H₄OC₂H₄OC₂H₄SO₃Na 3 —CONH—(C₂H₄O)₂C₂H₄SO₃Na1

In the Table, introduction sites of respective substituents of (R₁) and(R₂) are in an irregular order within the β-position substitution type[showing isomers represented by formulae (a)-1 to (a)-4]. The value of kand l are a charging ratio (eq./eq.) of the phthalonitrile derivativeused in the synthesis of the phthalocyanine derivative.

In Table 11 below, formula (XX-3) represents a (k+l+m)-valentphthalocyanine nucleus (the introduction site of the substituent R isthe β-position substitution type defined in the present invention), Rrepresents R₁ and/or R₂ and/or R₃, t represents a number of t=1 or 2, krepresents a number of 0<k<8, l represents a number of 0<l<8, and mrepresents a number of 0<m<8, provided that k, l and m each represents anumber satisfying 4≦k+l+m≦8.

TABLE 11 Formula (XX-3):

Compound No. M R₁ k R₂ l R₃ m 151 Cu —SO₂(CH₂)₃SO₃Li 2

1

1 152 Ni —SO₂(CH₂)₃SO₃Li 1 —SO₂(CH₂)₅CO₂Li 1

2 153 Cu —SO₂(CH₂)₃SO₃K 1.5

0.5 —SO₂(CH₂)₃SO₂NHC₂H₄OC₂H₄OH 2 154 Cu —SO₂(CH₂)₃SO₃Li 2

1

1 155 Zn —SO₂(CH₂)₃SO₃Li 2

1

1

In the Table, introduction sites of respective substituents of (R₁),(R₂) and (R₃) are in an irregular order within the β-positionsubstitution type [showing isomers represented by formulae (a)-1 to(a)-4]. The value of k, l and m are a charging ratio (eq./eq./eq.) ofthe phthalonitrile derivative used in the synthesis of thephthalocyanine derivative.

In Table 12 below, formula (XX-4) represents a (k+l+m+n)-valentphthalocyanine nucleus (the introduction site of the substituent R isthe β-position substitution type defined in the present invention), Rrepresents R₁ and/or R₂ and/or R₃ and/or R₄, t represents a number oft=1 or 2, k represents a number of 0<k<8, and 1 represents a number of0<l<8, m represents a member of 0<m<8, and n represents a number of0<n<8, provided that k, l, m and n each represents a number satisfying4≦k+l+m+n≦8.

TABLE 12 Formula (XX-4):

Compound No. M R₁ k R₂ l R₃ 156 Cu —SO₂(CH₂)₃SO₃Na 1 —SO₂(CH₂)₃CO₂Na 1

157 Cu —SO₂(CH₂)₃SO₃NH₄ 1 —SO₂(CH₂)₃CO₂NH₄ 1

158 Cu —SO₂(CH₂)₃SO₃K 1 —SO₂(CH₂)₃CO₂K 1

159 Cu —SO₂(CH₂)₃SO₃Li 1 —SO₂(CH₂)₃CO₂Li 1

160 Cu —SO₂(CH₂)₃SO₃K 1 —SO₂NH(CH₂)₃SO₃K 1

Compound No. m R₄ n 156 1

1 157 1

1 158 1

1 159 1

1 160 1

1

In the Table, introduction sites of respective substituents of (R₁),(R₂), (R₃) and (R₄) are in an irregular order within the β-positionsubstitution type [showing isomers represented by formulae (a)-1 to(a)-4]. The values of k, l, m and n are a charging ratio(eq./eq./eq./eq.) of the phthalonitrile derivative used in the synthesisof the phthalocyanine derivative.

The amount of the colorant added is preferably from 0.2 to 10 mass %,more preferably from 0.5 to 7 mass %, and most preferably from 1 to 5mass %, based on the ink composition.

The guanidine-based compound used together with the colorant in thepresent invention is described in detail below

(Guanidine-Based Compound)

The guanidine-based compound for use in the present invention means acompound having a structure of N—C(═N)—N.

The guanidine-based compound is preferably a compound represented byformula (1).

(wherein R₁₀₁, R₁₀₂, R₁₀₃ and R₁₀₄ each independently represents ahydrogen atom, an alkyl group, an alkoxy group, an aryl group, aheterocyclic group or an amino group, R₁₀₅ represents a hydrogen atom,an alkyl group, an alkoxy group, an aryl group or a heterocyclic group,and these alkyl group, alkoxy group, aryl group, heterocyclic group andamino group each may be substituted or unsubstituted).

The alkyl group is preferably an alkyl group having a carbon number of 1to 12, more preferably an alkyl group having a carbon number of 1 to 6.

The alkoxy group is preferably an alkoxy group having a carbon number of1 to 12, more preferably an alkoxy group having a carbon number of 1 to6.

The aryl group is preferably an aryl group having a carbon number of 6to 18, more preferably an aryl group having a carbon number of 6 to 10.

Examples of the heterocyclic group include a furyl group, a pyridylgroup, a pyrimidyl group, a pyrrolyl group, a pyrrolinyl group, apyrrolidyl group, a dioxolyl group, a pyrazolyl group, a pyrazolynylgroup, a pyrazolidyl group, an imidazolyl group, an oxazolyl group, athiazolyl group, an oxadiazolyl group, a triazolyl group, a thiadiazolylgroup, a pyryl group, a pyridyl group, a piperidyl group, a dioxanylgroup, a morpholyl group, a pyridazyl group, a pyrazyl group, apiperazyl group, a triazyl group and a trithianyl group.

The alkyl group, alkoxy group, aryl group and heterocyclic grouprepresented by R₁₀₁ to R₁₀₅ include those where the hydrogen atom isfurther substituted by another arbitrary substituent. Examples of such asubstituent include a halogen atom such as chlorine, a nitro group, anamino group, a carboxyl group, a hydroxyl group, a carbamoyl group, anamidino group, a guanidino group and an aryloxy group (the aryl moietymay be further substituted by a substituent enumerated here). Two ormore kinds of these substituents may be substituted in the samemolecule. Also, in the amino group, carbamoyl group, amidino group andguanidino group, the hydrogen atom may be substituted by an alkyl group,alkoxy group, aryl group or heterocyclic group represented by R₁₀₁ toR₁₀₅.

In the amino group represented by R₁₀₁ to R₁₀₄, the hydrogen atom may besubstituted by an alkyl group, alkoxy group, aryl group or heterocyclicgroup represented by R₁₁₀ to R₁₀₅.

The guanidine-based compound may be in the form of a salt or a metalcomplex. Examples thereof include hydrochloride, nitrate, phosphate,sulfamate, carbonate and acetate.

The guanidine-based compound include those shown below, and these may beused individually or in combination, but the present invention is notlimited thereto.

As for the synthesis method of the compound represented by formula (1),the compound can be obtained, for example, by passing through at least astep of causing ammonia to act on a hydrochloride of the correspondingimino ether.

The guanidine-based compound may be a polymer having an N—C(═N)—Nstructure. Such a polymer includes, but is not limited to, a compoundcontaining a repeating unit represented by the following formula (2-Aa),(2-Ab) or (2-Ac). The compound containing this repeating unit may be anoligomer. Also, the compound containing a repeating unit represented byformula (2-Ac) may be a monomer. These compounds are preferably a saltwith an acid.

In formula (2-Aa), R₁₀₅ has the same meaning as above, R₁₀₆ representsany one of R₁₀₁, R₁₀₂, R₁₀₃ and R₁₀₄, and the n-number of R₁₀₅'s orR₁₀₆'s may be the same or different n is an integer of 2 or more and ispreferably an integer of 2 to 30, more preferably from 2 to 15.

The compound containing a repeating unit represented by formula (2-Aa)may be a homopolymer or a copolymer with another repeating unit such asazetidinium, The terminal structure may be appropriately selected but ispreferably a hydrogen atom, an alkyl group, an alkoxy group, an arylgroup, a heterocyclic group or an amino group.

In formula (2-Ab), R₁₀₅ and R₁₀₆ have the same meanings as above, andthe 1-number of R₁₀₅'s or R₁₀₆'s may be the same or different. 1represents an integer of 2 or more and is preferably an integer of 2 to10, more preferably from 2 to 5. m represents an integer of 1 or moreand is preferably an integer of 1 to 6, more preferably from 1 to 3. Thecompound containing a repeating unit represented by formula (2-Ab) maybe a homopolymer or a copolymer with another repeating unit such asazetidinium, The terminal structure may be appropriately selected but ispreferably a hydrogen atom, an alkyl group, an alkoxy group, an arylgroup, a heterocyclic group or an amino group.

In formula (2-Ac), R₁₀₅ has the same meanings as above, R₁₀₇ has thesame meaning as R₁₀₁ or R₁₀₂, R₁₀₈ has the same meaning as R₁₀₄ or R₁₀₅,and the p-number of R₁₀₃'s, R₁₀₇'s or R₁₀₈'s may be the same ordifferent. p represents an integer of 1 or more and is preferably aninteger of 1 to 10, more preferably from 1 to 5. The compound containinga repeating unit represented by formula (2-Ac) may be a homopolymer or acopolymer with another repeating unit such as azetidinium. The terminalstructure may be appropriately selected but is preferably a hydrogenatom, an alkyl group, an alkoxy group, an aryl group, a heterocyclicgroup or an amino group.

The total amount added of at least one kind of a guanidine-basedcompound is preferably from 0.1 to 10 mass %, more preferably from 0.3to 7 mass %, and most preferably from 0.5 to 5 mass %, based on the inkcomposition.

The colorant/guanidine-based compound (mass ratio) is preferably from0.01 to 100, more preferably from 0.1 to 50, still more preferably from0.3 to 10.

The colorless water-soluble planar compound having more than tendelocalized π-electrons within one molecule, which is used together withthe colorant in the present invention, is described below.

When the number of π-electrons constituting a delocalized π-electronsystem is increased and the π-electron system is broadened, the inkcomposition comes to have absorption in the visible region in manycases. The term “colorless” as used in the present invention includes astate that the compound is very slightly colored within the range of notaffecting the image. The compound may be a fluorescent compound but ispreferably a compound having no fluorescence, more preferably a compoundwhere λmax having the absorption peak on the longest wave side is 350 nmor less, preferably 320 nm or less, and at the same time, the molarabsorption coefficient is 10,000 or less.

The compound for use in the present invention has more than tendelocalized π-electrons within one molecule. The number of π-electronsis not particularly limited in its upper limit but is preferably 80 orless, more preferably 50 or less, still more preferably 30 or less.Also, more than ten π-electrons may form one large delocalized systembut may form two or more delocalized systems. In particular, a compoundhaving two or more aromatic rings within one molecule is preferred. Thearomatic ring may be an aromatic hydrocarbon ring or an aromatic heteroring containing a heteroatom or may be ring-condensed to form onearomatic ring. Examples of the aromatic ring include benzene,naphthalene, anthracene, pyridine, pyrimidine, pyrazine and triazine.

The water-soluble planar compound for use in the present invention ispreferably a compound which dissolves in an amount of at least 1 g, morepreferably 5 g of more, most preferably 10 g or more, per 100 g of waterat 20° C.

In the case of a compound having two or more aromatic rings within onemolecule, the compound preferably has at least two solubilizing groupsbonded to the aromatic ring in the molecule. Examples of the usefulsolubilizing group include, but are not limited to, a sulfo group, acarboxyl group, a hydroxy group, a phosphono group, a carbonamido group,a sulfonamido group, a quaternary ammonium salt and other groups knownto one skilled in the art. Among these, a sulfo group and a carboxylgroup are preferred, and a sulfo group is most preferred.

The maximum number of solubilizing groups in the molecule is limitedonly by the number of usable positions of the substituent, but for thepractical purpose, it may suffice if ten same or different solubilizinggroups are present in the molecule. The counter cation of thesolubilizing group is not limited. The counter cation includes an alkalimetal, ammonium and an organic cation (e.g., tetramethylammonium,guanidinium, pyridinium), Among them, an alkali metal and ammonium arepreferable, lithium, sodium, potassium and ammonium are especiallypreferable, and lithium, sodium, ammonium are the most preferable.

Specific examples of the compound include the compounds described inJP-A-63-55544, JP-A-3-146947, JP-A-3-149543, JP-A-2001-201831,JP-A-2002-139822, JP-A-2002-196460, JP-A-2002-244257, JP-A-2002-244259,JP-A-2002-296743, JP-A-2002-296744, JP-A-2003-255502, JP-A-2003-307823,JP-A-2004-4500 and JP-A-2004-170964.

Above all, a compound represented by the following formula (3) ispreferred.A-X-L-(Y—B)_(n)  Formula (3)

In the formula, A, L and B each independently represents an aromaticgroup (including an aryl group and an aromatic heterocyclic group). Xand Y each independently represents a divalent linking group, nrepresents 0 or 1. The aromatic group may be monocyclic or a condensedring. The divalent linking group is an alkylene group, an alkenylenegroup, —CO—, —SO_(n)— (n is 0, 1 or 2), —NR— (R represents a hydrogenatom, an alkyl group, an aryl group or a heterocyclic group), —O—, or adivalent group comprising a combination of these linking groups.However, the compound represented by formula (3) contains at least oneionic hydrophilic group selected from a sulfo group, a carboxyl group, aphenolic hydroxyl group and a phosphono group. The ionic hydrophilicgroup may be in the form of a salt, and the counter cation thereof isnot limited. The counter cation includes an alkali metal, ammonium andan organic cation (e.g., tetramethylammonium, guanidinium, pyridinium)and is preferably an alkali metal or ammonium, more preferably lithium,sodium, potassium or ammonium, and most preferably lithium, sodium orammonium.

The compound represented by formula (3) may have a substituent otherthan an ionic hydrophilic group, and specific examples of thesubstituent include an alkyl group, an aryl group, an aralkyl group, aheterocyclic group, an alkoxy group, an aryloxy group, a hydroxyl group,an amino group (including an anilino group and a heterocyclic aminogroup), an acyl group, an acylamino group, a ureido group, a halogenatom, a sulfamoyl group, a carbamoyl group, a sulfonamido group, asulfonyl group, a sulfenyl group and a sulfinyl group, These groups eachmay further have a substituent. Among the compounds of formula 3, acompound where n=1 or where at least one of A, L and B is an aromatichetero ring is preferred, and a compound containing from two to fourionic hydrophilic groups is more preferred

The amount used of the colorless water-soluble planar compound havingmore than ten delocalized π-electrons within one molecule for use in thepresent invention is preferably from 0.01 to 10 mass %, more preferablyfrom 0.1 to 7.0 mass %, and most preferably from 0.5 to 5.0 mass %,based on the ink.

The colorant/planar compound (mass ratio) is preferably from 0.02 to1,000, more preferably from 0.1 to 100, still more preferably from 0.2to 50.

If the amount used is small, the ability of preventing bronze/improvingfastness to ozone gas may be insufficient.

If the amount used is large, the ejection property may be worsened.

The operation mechanism by which the compound of the present inventionprevents bronze is not clearly known, but it is considered that thecompound acts as a disaggregating agent of eliminating aggregation bycausing the π-electron to exert a stronger interaction on the coloringmatter aggregated (associated) by the π-electron interaction betweenmolecules of the coloring matter and the bronze phenomenon is therebyimproved. In order to intrude between aggregated coloring matters orexert a strong π-electron interaction on the coloring matter present inthe surface of the coloring matter aggregate, it is important that thedisaggregating agent is planar and the π-electron system is largelybroadened. Furthermore, in order to cause no precipitation of thedisaggregating agent itself or a complex formed by the coloring matterand the disaggregating agent, it is also important that thedisaggregating agent has sufficiently high solubility, The necessarynumber of π-electrons greatly varies depending on the coloring matterused for the inkjet ink, but since the coloring matter used for theinkjet ink has a largely extended planar structure for increasing thefixing property as represented by the direct dye, it is presumed thatthe disaggregating agent needs to be a colorless water-soluble planarcompound having a system of more than ten delocalized π-electrons withinone molecule. In addition, the complex formed by the disaggregatingagent and the coloring matter takes a form of protecting the coloringmatter with the disaggregating agent and therefore, the resistanceagainst ozone gas is also enhanced.

Preferred examples of the compound for use in the present inventioninclude the compounds described in JP-A-2002-139822, JP-A-2002-196460,JP-A-2002-244257, JP-A-2002-244259, JP-A-2002-296743 andJP-A-2002-296744, supra. Representative compounds (disaggregating agent)are set forth below.

Preferred compounds for use in the present invention can be easilysynthesized by referring to, for example, JP-A-2002-139822, supra,

The intended end-usage of the ink composition of the present inventionincludes an image recording material for forming an image, particularly,a color image. Specific examples thereof include an inkjet recordingmaterial which is described in detail later, a heat-sensitive recordingmaterial, a pressure-sensitive recording material, a recording materialfor use with an electrophotographic system, a transfer-type silverhalide light-sensitive material, a printing ink and a recording pen.Among these, preferred are an inkjet recording material, aheat-sensitive recording material and a recording material for use withan electrophotographic system, more preferred is an inkjet recordingmaterial.

The ink composition of the present invention may also be applied to adyeing solution for dyeing a color filter used to record/reproduce acolor image in a solid-state image sensor (e.g., CCD) or a display(e.g., LCD, PDP), or various fibers.

[Ink]

The ink composition of the present invention means an ink compositioncomprising at least one colorant of the present invention, water, aguanidine-based compound, and a colorless water-soluble planer compoundhaving more than ten delocalized π-electrons within one molecule.

The ink composition of the present invention may contain a medium andwhen the medium used is a solvent, the ink composition is suitableparticularly as an inkjet recording ink.

The ink composition of the present invention can be produced by using alipophilic medium or an aqueous medium as the medium and dissolvingand/or dispersing the colorant of the present invention therein

In the present invention, an aqueous medium is used, and a water-solubleink composition is preferred.

The ink of the present invention may contain, if desired, otheradditives within the range of not impairing the effects of the presentinvention.

Examples of other additives include known additives (described inJP-A-2003-306623) such as drying inhibitor (wetting agent),discoloration inhibitor, emulsification stabilizer, penetrationaccelerator, ultraviolet absorbent, antiseptic, fungicide, pH adjustingagent, surface tension adjusting agent, defoaming agent, viscosityadjusting agent, dispersant, dispersion stabilizer, rust inhibitor andchelating agent.

In the case of a water-soluble ink, these various additives are addeddirectly to the ink solution. In the case of using an oil-soluble dye inthe form of a dispersion, the additives are generally added to thedispersion after the preparation of a dye dispersion but may be added tothe oil or aqueous phase during the preparation.

The drying inhibitor is suitably used for the purpose of preventingclogging due to drying of the inkjet ink at the ink ejection port of anozzle in the inkjet recording system.

The drying inhibitor is preferably a water-soluble organic solventhaving a vapor pressure lower than water. Specific examples thereofinclude polyhydric alcohols as represented by ethylene glycol, propyleneglycol, diethylene glycol, polyethylene glycol, thiodiglycol,dithiodiglycol, 2-methyl-1,3-propanediol, 1,2,6-hexanetriol, acetyleneglycol derivative, glycerin and trimethylolpropane; lower alkyl ethersof polyhydric alcohol, such as ethylene glycol monomethyl(orethyl)ether, diethylene glycol monomethyl(or ethyl)ether and triethyleneglycol monoethyl(or butyl)ether; heterocyclic rings such as2-pyrrolidone, N-methyl-2-pyrrolidone, 1,3-dimethyl-2-imidazolidinoneand N-ethylmorpholine; sulfur-containing compounds such as sulfolane,dimethylsulfoxide and 3-sulfolene; polyfunctional compounds such asdiacetone alcohol and diethanolamine; and urea derivatives. Among these,polyhydric alcohols such as glycerin and diethylene glycol arepreferred. These drying inhibitors may be used individually or incombination of two or more thereof. In the ink, the drying inhibitor ispreferably contained in an amount of 10 to 50 mass %.

The penetration accelerator is suitably used for the purpose of moresuccessfully penetrating the inkjet recording ink into paper. Examplesof the penetration accelerator which can be used include alcohols suchas ethanol, isopropanol, butanol, di(tri)ethylene glycol monobutyl etherand 1,2-hexanediol, sodium laurylsulfate, sodium oleate and nonionicsurfactants. A sufficiently high effect can be usually obtained byadding from 5 to 30 mass % of the penetration accelerator in the ink.The penetration accelerator is preferably used in an amount of causingno blurring of printed letter or no print through.

The ultraviolet absorbent is used for the purpose of enhancing thepreservability of image. Examples of the ultraviolet absorbent which canbe used include benzotriazole-base compounds described inJP-A-58-185677, JP-A-61-190537, JP-A-2-782, JP-A-5-197075 andJP-A-9-34057, benzophenone-base compounds described in JP-A-46-2784,JP-A-5-194483 and U.S. Pat. No. 3,214,463, cinnamic acid-based compoundsdescribed in JP-B-48-30492 (the term “JP-B” as used herein means an“examined Japanese patent publication”), JP-B-56-21141 andJP-A-10-88106, triazine-base compounds described in JP-A-4-298503,JP-A-8-53427, JP-A-8-239368, JP-A-10-182621 and JP-T-8-501291 (the term“JP-T” as used herein means a “published Japanese translation of a PCTpatent application”), compounds described in Research Disclosure No.24239, and compounds of absorbing ultraviolet light and emittingfluorescent light, so-called fluorescent brightening agents, asrepresented by a stilbene-based compound and a benzoxazole-basedcompound.

The discoloration inhibitor is used for the purpose of enhancing thepreservability of image. As the discoloration inhibitor, various organicor metal complex-based discoloration inhibitors can be used. Examples ofthe organic discoloration inhibitor include hydroquinones,alkoxyphenols, dialkoxyphenols, phenols, anilines, amines, indanes,chromans, alkoxyanilines and hetero rings. Examples of the metal complexinclude a nickel complex and a zinc complex. More specifically,compounds described in patent documents cited in Research Disclosure,Nos. 17643 (Items VII-I to VII-J), 15162, 18716 (page 650, left column),36544 (page 527), 307105 (page 872) and 15162, and compounds included informulae of representative compounds and in exemplary compoundsdescribed in JP-A-62-215272 (pages 127 to 137) can be used.

Examples of the fungicide include sodium dehydroacetate, sodiumbenzoate, sodium pyridinethione-1-oxide, ethyl p-hydroxybenzoate,1,2-benzisothiazolin-3-one and salts thereof. In the ink, the fungicideis preferably used in an amount of 0.02 to 1.00 mass %.

As the pH adjusting agent, a neutralizer (e.g., organic base, inorganicalkali) described above may be used. The pH adjusting agent is used forthe purpose of enhancing the storage stability of the inkjet recordingink. The pH adjusting agent is preferably added so that the inkjetrecording ink can be used in summer, that is, can have a pH of 6 to 10,more preferably a pH of 7 to 10.

Examples of the surface tension adjusting agent include nonionic,cationic and anionic surfactants. The surface tension of the inkjetrecording ink of the present invention is preferably from 25 to 70mPa·s, more preferably from 25 to 60 mPa·s. Also, the viscosity of theinkjet recording ink of the present invention is preferably 30 mPa·s orless. The viscosity is more preferably adjusted to 20 mPa·s or less.

Preferred examples of the surfactant include an anionic surfactant suchas fatty acid salt, alkylsulfuric ester salt, alkylbenzenesulfonate,alkylnaphthalenesulfonate, dialkylsulfosuccinate, alkylphosphoric estersalt, naphthalenesulfonic acid formalin condensate andpolyoxyethylenealkylsulfuric ester salt, and a nonionic surfactant suchas polyoxyethylene alkyl ether, polyoxyethylene alkylallyl ether,polyoxyethylene fatty acid ester, sorbitan fatty acid ester,polyoxyethylene sorbitan fatty acid ester, polyoxyethylene alkylamine,glycerin fatty acid ester and oxyethylene oxypropylene block copolymer.

Also, SURFYNOLS (produced by Air Products & Chemicals), which are anacetylene-based polyoxyethylene oxide surfactant, may be preferablyused. Furthermore, an amine oxide-type amphoteric surfactant such asN,N-dimethyl-N-alkylamine oxide is also preferred. In addition, thosedescribed as the surfactant in JP-A-59-157636 (pages (37) to (38)) andResearch Disclosure, No 308119 (1989) may also be used.

A defoaming agent such as fluorine- or silicone-base compound orchelating agent as represented by EDTA may be also used, if desired.

In the case of dispersing the colorant for use in the present inventionin an aqueous medium, it is preferred that a colored fine particlecontaining a coloring matter and an oil-soluble polymer is dispersed inan aqueous medium as described in JP-A-11-286637, JP-A-2001-240763,JP-A-2001-262039 and JP-A-2001-247788, or the colorant of the presentinvention dissolved in a high-boiling point organic solvent is dispersedin an aqueous medium as described in JP-A-2001-262018, JP-A-2001-240763,JP-A-2001-335734 and JP-A-2002-80772.

As regards the specific method for dispersing the colorant of thepresent invention in an aqueous medium, the oil-soluble polymer,high-boiling point organic solvent and additives used, and the amountsthereof, those described in the patent publications above may bepreferably employed.

At the time of dispersing the colorant, a dispersant and a surfactantmay be used. As for the dispersing device, a simple stirrer or impellerstirring system, an inline stirring system, a mill system (e.g., colloidmill, ball mill, sand mill, attritor, roll mill, agitator mill), anultrasonic wave system, and a high-pressure emulsion dispersion system(a high-pressure homogenizer; specific examples of the commerciallyavailable device include a Gaulin homogenizer, Microfluidizer and DeBEE2000) may be employed.

Details of the preparation process of the inkjet recording ink aredescribed, other than the patent publications above, in JP-A-5-148436,JP-A-5-295312, JP-A-7-97541, JP-A-7-82515, JP-A-7-118584, JP-A-11-286637and JP-A-2001-271003, and these can be utilized also in the preparationof the inkjet recording ink of the present invention.

The aqueous medium mainly comprises water and if desired, a mixturewhere a water-miscible organic solvent is added can be used. Examples ofthe water-miscible organic solvent include alcohols (e.g., methanol,ethanol, propanol, isopropanol, butanol, isobutanol, sec-butanol,tert-butanol, pentanol, hexanol, cyclohexanol, benzyl alcohol),polyhydric alcohols (e.g., ethylene glycol, diethylene glycol,triethylene glycol, polyethylene glycol, propylene glycol, dipropyleneglycol, polypropylene glycol, butylene glycol, hexanediol, pentanediol,glycerin, hexanetriol, thiodiglycol), glycol derivatives (e.g., ethyleneglycol monomethyl ether, ethylene glycol monoethyl ether, ethyleneglycol monobutyl ether, diethylene glycol monomethyl ether, diethyleneglycol monobutyl ether, propylene glycol monomethyl ether, propyleneglycol monobutyl ether, dipropylene glycol monomethyl ether, triethyleneglycol monomethyl ether, ethylene glycol diacetate, ethylene glycolmonomethyl ether acetate, triethylene glycol monomethyl ether,triethylene glycol monoethyl ether, ethylene glycol monophenyl ether),amines (e.g., ethanolamine, diethanolamine, triethanolamine,N-methyldiethanolamine, N-ethyldiethanolamine, morpholine,N-ethylmorpholine, ethylenediamine, diethylenetriamine,triethylenetetramine, polyethyleneimine, tetramethylpropylenediamine)and other polar solvents (e.g., formamide, N,N-dimethylformamide,N,N-dimethylacetamide, dimethylsulfoxide, sulfolane, 2-pyrrolidone,N-methyl-2-pyrrolidone, N-vinyl-2-pyrrolidone, 2-oxazolidone,1,3-dimethyl-2-imidazolidinone, acetonitrile, acetone), Thesewater-miscible organic solvents may be used in combination of two ormore thereof.

In the inkjet recording ink of the present invention, the colorant ispreferably contained in an amount of 0.1 to 10 parts by mass per 100parts by mass of the inkjet recording ink.

In the inkjet recording ink of the present invention, another coloringagent may be used in combination with the colorant of the presentinvention represented by formulae (I) and (IV).

In the case of using two or more colorants in combination, the totalcontent of colorants is preferably in the above-described range.

The inkjet recording ink of the present invention can be used not onlyfor the formation of a monochromatic image but also for the formation ofa full color image.

For forming a full color image, a magenta color tone ink, a cyan colortone ink and a yellow color tone ink can be used. Also, for adjustingthe color tone, a black color tone ink may be further used In theseinks, other coloring materials (dye or pigment) may also be used inaddition to the colorant according to the present invention so as toenhance the image reproducing performance.

The yellow dye which can be used together with the colorant of thepresent invention may be an arbitrary yellow dye. Examples thereofinclude an aryl- or heteryl-azo dye having phenols, naphthols, anilines,hetero rings (e.g., pyrazolone, pyridone), open chain-type activemethylene compounds or the like as the coupling component (hereinafterreferred to as a “coupler component”); an azomethine dye having openchain-type active methylene compounds or the like as the couplercomponent; a methine dye such as benzylidene dye and monomethine oxonoldye; and a quinone-based dye such as naphthoquinone dye andanthraquinone dye. Other examples of the dye species include aquinophthalone dye, a nitro•nitroso dye, an acridine dye and anacridinone dye.

The magenta dye which can be used may be an arbitrary magenta dye.Examples thereof include an aryl- or heteryl-azo dye having phenols,naphthols, anilines or the like as the coupler component, an azomethinedye having pyrazolones, pyrazolotriazoles or the like as the couplercomponent; a methine dye such as arylidene dye, styryl dye, merocyaninedye, cyanine dye and oxonol dye; a carbonium dye such as diphenylmethanedye, triphenylmethane dye and xanthene dye; a quinone dye such asnaphthoquinone, anthraquinone and anthrapyridone; and a condensedpolycyclic dye such as dioxazine dye.

The cyan dye which can be used may be an arbitrary cyan dye. Examplesthereof include an aryl- or heteryl-azo dye having phenols, naphthols,anilines or the like as the coupler component; an azomethine dye havingphenols, naphthols, hetero rings (e.g., pyrrolotriazole) or the like asthe coupler component; a polymethine dye such as cyanine dye, oxonol dyeand merocyanine dye; a carbonium dye such as diphenylmethane dye,triphenylmethane dye and xanthene dye; a phthalocyanine dye which is notrepresented by the formula (I) or (IV) in the invention; ananthraquinone dye; and an indigo•thioindigo dye.

These dyes may be a dye which provides a yellow, magenta or cyan colorfor the first time when a part of the chromophore is dissociated. Inthis case, the counter cation may be an inorganic cation such as alkalimetal and ammonium, an organic cation such as pyridinium and quaternaryammonium salt, or a polymer cation having such a cation in a partialstructure.

Examples of the black coloring material which can be used includedis-azo, tris-azo and tetra-azo dyes and a dispersion of carbon black.

[Inkjet Recording Method]

In the inkjet recording method of the present invention, an energy issupplied to the above-described inkjet recording ink and thereby animage is formed on a known image-receiving material, namely, plainpaper, resin coated paper, inkjet special paper described, for example,in JP-A-8-169172, JP-A-8-27693, JP-A-2-276670, JP-A-7-276789,JP-A-9-323475, JP-A-62-238783, JP-A-10-153989, JP-A-10-217473,JP-A-10-235995, JP-A-10-337947, IP-A-10-217597 and JP-A-10-337947, film,electrophotographic common paper, cloth, glass, metal, ceramic or thelike.

At the formation of an image, a polymer latex compound may be used incombination for the purpose of giving glossiness or water resistance orimproving the weather resistance.

The timing of imparting the latex compound to the image-receivingmaterial may be before, after or simultaneous with the addition of thecolorant. Accordingly, the site to which the polymer latex is added maybe in the image-receiving paper or ink, or a liquid material of thepolymer latex alone may be prepared and used. More specifically, themethods described in JP-A-2002-166638, JP-A-2002-121440,JP-A-2002-154201, JP-A-2002-144696, JP-A-2002-80759, JP-A-2002-187342and JP-A-2002-172774 may be preferably used.

The recording paper and recording film which are used in performing theinkjet printing by using the ink of the present invention are describedbelow.

The support which can be used for the recording paper or film isproduced, for example, from a chemical pulp such as LBKP and NBKP, amechanical pulp such as GP, PGW, RMP, TMP, CTMP, CMP and CGP, or a wastepaper pulp such as DIP, by mixing, if desired, conventionally knownadditives such as pigment, binder, sizing agent, fixing agent, cationagent and paper strength increasing agent, and then sheeting the mixtureby using various devices such as Fourdrinier paper machine and cylinderpaper machine. Other than these supports, synthetic paper or plasticfilm may be used. The thickness of the support is preferably from 10 to250 μm, and the basis weight is preferably from 10 to 250 g/m². Anink-receiving layer and a backcoat layer may be provided on the supportas it is or after providing a size press or anchor coat layer by usingstarch, polyvinyl alcohol or the like, an ink-receiving layer and abackcoat layer may be provided The support may be further subjected to aflattening treatment by a calendering device such as machine calender,TG calender and soft calender. The support for use in the presentinvention is preferably paper or plastic film of which both surfaces arelaminated with a polyolefin (for example, polyethylene, polystyrene,polyethylene terephthalate, polybutene or a copolymer thereof). In thepolyolefin, a white pigment (e.g., titanium oxide, zinc oxide) or atinting dye (e.g., cobalt blue, ultramarine, neodymium oxide) ispreferably added.

The ink-receiving layer provided on the support contains a pigment andan aqueous binder. The pigment is preferably a white pigment Examples ofthe white pigment include an inorganic white pigment such as calciumcarbonate, kaolin, talc, clay, diatomaceous earth, synthetic amorphoussilica, aluminum silicate, magnesium silicate, calcium silicate,aluminum hydroxide, alumina, lithopone, zeolite, barium sulfate, calciumsulfate, titanium dioxide, zinc sulfide and zinc carbonate, and anorganic pigment such as styrene-based pigment, acryl-based pigment, urearesin and melamine resin. The white pigment contained in theink-receiving layer is preferably a porous inorganic pigment, morepreferably a synthetic amorphous silica or the like having a large porearea. The synthetic amorphous silica may be either a silicic acidanhydride obtained by a dry production process or a silicic acid hydrateobtained by a wet production process but is preferably a silicic acidhydrate.

Examples of the aqueous binder contained in the ink-receiving layerinclude a water-soluble polymer such as polyvinyl alcohol,silanol-modified polyvinyl alcohol, starch, cationized starch, casein,gelatin, carboxymethyl cellulose, hydroxyethyl cellulose,polyvinylpyrrolidone, polyalkylene oxide and polyalkylene oxidederivative, and a water-dispersible polymer such as styrene butadienelatex and acryl emulsion. These aqueous binders may be used individuallyor in combination of two or more thereof. Among these, polyvinyl alcoholand silanol-modified polyvinyl alcohol are preferred in the presentinvention in view of adhesion to the pigment and separation resistanceof the ink-receiving layer.

The ink-receiving layer may contain a mordant, a water-proofing agent, alight fastness enhancer, a surfactant and other additives in addition tothe pigment and the aqueous binder.

The mordant added to the ink-receiving layer is preferably immobilizedand for this purpose, a polymer mordant is preferably used.

The polymer mordant is described in JP-A-48-28325, JP-A-54-74430,JP-A-54-124726, JP-A-55-22766, JP-A-55-142339, JP-A-60-23850,JP-A-60-23851, JP-A-60-23852, JP-A-60-23853, JP-A-60-57836,JP-A-60-60643, JP-A-60-118834, JP-A-60-122940, JP-A-60-122941,JP-A-60-122942, JP-A-60-235134, JP-A-1-161236 and U.S. Pat. Nos.2,484,430, 2,548,564, 3,148,061, 3,309,690, 4,115,124, 4,124,386,4,193,800, 4,273,853, 4,282,305 and 4,450,224. An image-receivingmaterial containing the polymer mordant described in JP-A-1-161236(pages 212 to 215) is particularly preferred When the polymer mordantdescribed in this patent publication is used, an image having excellentimage quality can be obtained and at the same time, light fastness ofthe image is improved.

The water-proofing agent is effective for forming a water-resistantimage. The water-proofing agent is preferably a cationic resin Examplesof the cationic resin include polyamidopolyamine epichlorohydrin,polyethyleneimine, polyaminesulfone, poly-dimethyldiallylammoniumchloride, cation polyacrylamide and colloidal silica. Among thesecationic resins, polyamidopolyamine epichlorohydrin is preferred. Thecationic resin content is preferably from 1 to 15 mass %, morepreferably from 3 to 10 mass %, based on the entire solid content of theink-receiving layer.

Examples of the light fastness enhancer include zinc sulfate, zincoxide, a hindered amine-based antioxidant and a benzophenone-based orbenzotriazole-based ultraviolet absorbent. Among these, zinc sulfate ispreferred.

The surfactant functions as a coating aid, a releasability improver, aslipperiness improver or an antistatic agent The surfactant is describedin JP-A-62-173463 and JP-A-62-183457. In place of the surfactant, anorganofluoro compound may be used. The organofluoro compound ispreferably hydrophobic. Examples of the organofluoro compound include afluorine-containing surfactant, an oily fluorine-base compound (forexample, fluorine oil) and a solid fluorine compound resin (for example,ethylene tetrafluoride resin), The organofluoro compound is described inJP-B-57-9053 (columns 8 to 17), JP-A-61-20994 and JP-A-62-135826 Otherexamples of the additive added to the ink-receiving layer include apigment dispersant, a thickener, a defoaming agent, a coloring matter, afluorescent brightening agent, an antiseptic, a pH adjusting agent, amatting agent and a hardening agent The ink-receiving layer may becomposed of either one layer or two layers.

In the recording paper or film, a backcoat layer may also be provided.The component which can be added to this layer includes a white pigment,an aqueous binder and other components, Examples of the white pigmentcontained in the backcoat layer include an inorganic white pigment suchas precipitated calcium carbonate, heavy calcium carbonate, kaolin,talc, calcium sulfate, barium sulfate, titanium dioxide, zinc oxide,zinc sulfide, zinc carbonate, satin white, aluminum silicate,diatomaceous earth, calcium silicate, magnesium silicate, syntheticamorphous silica, colloidal silica, colloidal alumina, pseudo-boehmite,aluminum hydroxide, alumina, lithopone, zeolite, hydrolyzed halloysite,magnesium carbonate and magnesium hydroxide, and an organic pigment suchas styrene-based plastic pigment, acryl-based plastic pigment,polyethylene, microcapsule, urea resin and melamine resin.

Examples of the aqueous binder contained in the backcoat layer include awater-soluble polymer such as styrene/maleate copolymer,styrene/acrylate copolymer, polyvinyl alcohol, silanol-modifiedpolyvinyl alcohol, starch, cationized starch, casein, gelatin,carboxymethyl cellulose, hydroxyethyl cellulose andpolyvinylpyrrolidone, and a water-dispersible polymer such as styrenebutadiene latex and acryl emulsion. Other examples of the componentcontained in the backcoat layer include a defoaming agent, a foaminhibitor, a coloring matter, a fluorescent brightening agent, anantiseptic and a water-proofing agent.

A polymer latex may be added to a constituent layer (including thebackcoat layer) of the inkjet recording paper or film.

The polymer latex is used for the purpose of improving film physicalproperties, for example, stabilizing the dimension and preventing thecurling, adhesion or film cracking, The polymer latex is described inJP-A-62-245258, JP-A-62-1316648 and JP-A-62-110066. When a polymer latexhaving a low glass transition temperature (40° C. or less) is added to alayer containing a mordant, the layer can be prevented from cracking orcurling. The curling can also be prevented by adding a polymer latexhaving a high glass transition temperature to the backcoat layer.

The ink of the present invention is not limited in the inkjet recordingsystem and is used for a known system, for example, a charge controllingsystem of jetting out the ink by using an electrostatic induction force,a drop-on-demand system (pressure pulse system) utilizing a vibrationpressure of a piezoelectric element, an acoustic inkjet system ofconverting an electric signal into an acoustic beam, irradiating thebeam on the ink and jetting out the ink by using the radiation pressure,and a thermal inkjet system of heating the ink to form a bubble andutilizing the pressure generated. The inkjet recording system includes asystem of ejecting a large number of small-volume ink droplets of aso-called photo-ink having a low concentration, a system of improvingthe image quality by using a plurality of inks having substantially thesame color hue but differing in the concentration, and a system of usinga colorless transparent ink.

EMBODIMENT

The present invention is described in greater detail below by referringto Examples, but the present invention is not limited thereto.

(Ink C-1)

Ultrapure water having a resistance value of 18 MΩ or more is added tothe following components to make 100 g, and the resulting solution isstirred for 1 hour under heating at 30 to 40° C. Thereafter, thesolution is filtered under reduced pressure through a microfilter havingan average pore size of 0.25 μm to prepare Cyan Ink Solution (C-1).

C-1:

Dye 110 4.7 g Urea 2.4 g Triethylene glycol 10.7 g  Triethylene glycolmonobutyl ether 9.1 g 1,2-Hexanediol 2.4 g 2-Pyrrolidone 3.5 g Glycerin11.8 g  Triethanolamine 0.5 g Proxel XL II 1.0 g Olfin E1010 1.0 g(Ink C-2)

Ink C-2 is prepared in the same manner as Ink C-1 except for replacing5.7 g of water in Ink C-1 with 5.7 g of a 17.5 wt % aqueous solution ofCompound P-3.

(Ink C-3)

Ink C-3 is prepared in the same manner as Ink C-1 except for replacing1.0 g of water in Ink C-1 with 10 g of aminoguanidine hydrochloride.

(Ink C-4)

Ink C-4 is prepared in the same manner as Ink C-1 except for replacing6.7 g of water in Ink C-1 with 5.7 g of a 17.5 wt % aqueous solution ofCompound P-3 and 1.0 g of aminoguanidine hydrochloride.

(Ink C-5)

Ink C-5 is prepared in the same manner as Ink C-4 except for replacingDye 110 in Ink C-4 with Comparative Coloring Matter a.

(Ink C-6)

Ink C-6 is prepared in the same manner as Ink C-4 except for replacingDye 110 in Ink C-4 with Comparative Coloring Matter b.

(Ink C-7)

Ink C-7 is prepared in the same manner as Ink C-4 except for replacing1.0 g of aminoguanidine hydrochloride in Ink C-4 with 1.0 g of guanidinehydrochloride.

(Ink C-8)

Ink C-8 is prepared in the same manner as Ink C-4 except for replacing1.0 g of aminoguanidine hydrochloride in Ink C-4 with 110 g ofN,N′-diaminoguanidine.

(Ink C-9)

Ink C-9 is prepared in the same manner as Ink C-1 except for replacing7.7 g of water in Ink C-1 with 5.7 g of a 17.5 wt % aqueous solution ofCompound P-3 and 2.0 g of aminoguanidine hydrochloride and replacing Dye110 with Dye 108.

(Ink C-10) Ink C-10 is prepared in the same manner as Ink C-1 except forreplacing 12.4 g of water in Ink C-1 with 11.4 g of a 17.5 wt % aqueoussolution of Compound P-3 and 1.0 g of aminoguanidine hydrochloride andreplacing Dye 110 with Dye 108.

(Inkjet Recording)

Inks 1 to 10 prepared above each is filled in a cyan ink cartridge of aninkjet printer, PM-A-700, manufactured by Seiko Epson Corp., and animage is printed on photographic paper, Crispia <KO-KOTAKU>, produced bySeiko Epson Corp. and subjected to various evaluations.

(Evaluation of Ozone Resistance)

A monochromatic step patch image is printed. When 24 hours is passedafter printing of this step patch image, the reflection density (Ci) ineach concentration region of the step patch portion is measured using anX-rite 310 densitometer including a Status A Filter as standardequipment. Subsequently, a discoloration test is performed by storingthis sample in an ozone fadeometer at an ozone concentration of 5 ppmfor 7 days. A commercially available apparatus of high-pressure chargingtype, to which an AC voltage of 5 kV is applied, is used as theozonizer, and the ozone gas concentration is set and controlled using anozone gas monitor (Model OZG-EM-01) manufactured by APPLICS.

After storage for 7 days, the image density is again measured todetermine the density (Cf) after storage, and the residual coloringmatter ratio [%]=(Cf/Ci)×100 is obtained to evaluate the ozoneresistance. A value at a reflection density Ci of 0.9 to 1.1 is employedas the residual coloring matter ratio.

The samples are rated on a five-stage scale, namely, rated A when theresidual coloring matter ratio is 85% or more, rated B when from 80% toless than 85%, rated C when from 75% to less than 80%, rated D when from70% to less than 75%, and rated E when less than 70%.

(Generation of Bronze Gloss)

The cyan Dmax part after printing in an environment of 30° C. and 80% RHis observed with an eye to confirm whether bronze is generated or not.

TABLE 13 Ozone Resistance Bronze Ink C-1 (Comparative Example) Dgenerated Ink C-2 (Comparative Example) C none Ink C-3 (ComparativeExample) B generated Ink C-4 (Invention) A none Ink C-5 (ComparativeExample) E none Ink C-6 (Comparative Example) E none Ink C-7 (Invention)A none Ink C-8 (Invention) A none Ink C-9 (Invention) A none Ink C-10(Invention) A none

Even when the image-receiving paper for use in the present invention ischanged to Inkjet Photo Gloss Paper “GASAI” produced by Fuji Photo FilmCo., Ltd. or PR101 produced by Canon Inc., the same effects as in theresults above are obtained.

INDUSTRIAL APPLICABILITY

According to the present invention, an inkjet recording ink capable offorming a color image excellent in the color reproduction, assured ofsufficiently high fastness to light, heat, humidity and active gas inthe environment and free from occurrence of a bronze phenomenon can beprovided. Furthermore, an inkjet recording method satisfying both theimprovement of bronze phenomenon of the recorded image and theimprovement of preservability of the recorded image at the same time ina high improvement level, and a method for preventing the occurrence ofa bronze phenomenon of an image and improving the preservability of animage can be provided.

The entire disclosure of each and every foreign patent application fromwhich the benefit of foreign priority has been claimed in the presentapplication is incorporated herein by reference, as if fully set forth.

1. An ink composition comprising: a colorant represented by thefollowing formula (I); water; a guanidine-based compound; and acolorless water-soluble planar compound having more than ten delocalizedπ-electrons within one molecule:

wherein, M represents a hydrogen atom, a metal atom, an oxide thereof, ahydroxide thereof or a halide thereof; k, l, m and n represent aninteger of 0≦k≦8, an integer of0≦1≦8, an integer of 0≦m≦8and an integerof0≦n≦8, respectively, provided that k, l, m and n satisfy 4≦k+1+m+n≦8;each of X₁, X₂, X₃ and X₄ represents a substituent selected from thegroup consisting of —SO—R₁, —S0₂—R₁, —SO₂NR₂R₃, —CONR₂R₃, —CO₂—R₁,—CO—R₁, a sulfo group and a salt thereof, a carboxyl group and a saltthereof, and a phosphono group and a salt thereof, provided that atleast one of X₁, X₂, X₃ and X₄ has an ionic hydrophilic group as asubstituent; R₁ represents a substituted or unsubstituted alkyl group, asubstituted or unsubstituted aryl group, or a substituted orunsubstituted heterocyclic group; R₂ represents a hydrogen atom, asubstituted or unsubstituted alkyl group, a substituted or unsubstitutedaryl group, or a substituted or unsubstituted heterocyclic group; R₃represents a hydrogen atom, a substituted or unsubstituted alkyl group,a substituted or unsubstituted aryl group, or a substituted orunsubstituted heterocyclic group; and Pc represents a (k+l+m+n)-valentphthalocyanine nucleus represented by the following formula (II);

wherein each of the four benzene rings A, B, C and D has at least one ofX₁, X₂, X₃ and X₄; and Y₁, Y₂, Y₃, Y₄, Y₅, Y₆, Y₇ and Y₈ eachindependently represents a hydrogen atom or a monovalent substituentwhich may further have a substituent.
 2. The ink composition accordingto claim 1, wherein the phthalocyanine nucleus represented by theformula (II) is represented by the following formula (III):


3. The ink composition according to claim 1, wherein the colorantrepresented by the formula (I) is represented by the following formula(IV):

wherein M represents a hydrogen atom, a metal atom, an oxide thereof, ahydroxide thereof or a halide thereof; k and l represent an integer of0<k<8 and an integer of 0<1<8, respectively, provided that k and 1satisfy 4≦k+1≦8; each of X₁ and X₂ represents a substituent selectedfrom the group consisting of —SO—R₁, —SO₂—R₁, —SO₂NR₂R₃, a sulfo groupand a salt thereof, provided that X₁ and X₂ are different from eachother and at least one of X_(l)and X₂, has an ionic hydrophilic group asa substituent; R₁ represents a substituted or unsubstituted alkyl group,a substituted or unsubstituted aryl group, or a substituted orunsubstituted heterocyclic group; R₂ represents a hydrogen atom, asubstituted or unsubstituted alkyl group, a substituted or unsubstitutedaryl group, or a substituted or unsubstituted heterocyclic group; R₃represents a hydrogen atom, a substituted or unsubstituted alkyl group,a substituted or unsubstituted aryl group, or a substituted orunsubstituted heterocyclic group; and Pc represents a (k+1)-valentphthalocyanine nucleus represented by the formula (III), wherein each ofthe four benzene rings A, B, C and D has at least one of X₁ and X₂. 4.The ink composition according to claim 1, wherein the water-solubleplanar compound has at least two aromatic rings.
 5. The ink compositionaccording to claim 1, wherein the water-soluble planar compound has nofluorescence, and has 350 nm or less of λmax and 10,000 or less of molarabsorption coefficient, wherein λmax represents a wavelength of theabsorption peak having the longest wavelength.
 6. The ink compositionaccording to claim 1, wherein the water-soluble planar compound has asulfo group.
 7. The ink composition according to claim 1, wherein theguanidine-based compound is represented by the following formula (1):

R₁₀₁, R₁₀₂, R₁₀₃ and R₁₀₄ each independently represents a hydrogen atom,a substituted or unsubstituted alkyl group, a substituted orunsubstituted alkoxy group, a substituted or unsubstituted aryl group, asubstituted or unsubstituted heterocyclic group, or substituted orunsubstituted an amino group; and R₁₀₅ represents a hydrogen atom, asubstituted or unsubstituted alkyl group, a substituted or unsubstitutedalkoxy group, a substituted or unsubstituted aryl group, or asubstituted or unsubstituted heterocyclic group.
 8. The ink compositionaccording to claim 1, wherein the guanidine-based compound is in anamount of 0.1 to 10 mass% based on the ink composition.
 9. The inkcomposition according to claim 1, further comprising: a surfactant. 10.The ink composition according to claim 9, wherein the surfactant is inan amount of 0.05 to 50 g/liter based on the ink composition.
 11. Theink composition according to claim 9, wherein the surfactant is anonionic surfactant.
 12. The ink composition according to claim 11,wherein the nonionic surfactant is an acetylene glycol-based surfactant.13. The ink composition according to claim 1, further comprising: anantiseptic.
 14. An inkjet recording ink prepared by utilizing the inkcomposition according to claim
 1. 15. An inkjet recording methodutilizing the inkjet recording ink according to claim 14.